An article DNA-Encoded Libraries: Hydrazide as a Pluripotent Precursor for On-DNA Synthesis of Various Azole Derivatives WOS:000644481700001 published article about ONE-POT SYNTHESIS; SOLID-PHASE SYNTHESIS; OXIDATIVE CYCLIZATION; 2,5-DISUBSTITUTED 1,3,4-OXADIAZOLES; 3,5-DISUBSTITUTED 1,2,4-TRIAZOLES; 1,3,4-THIADIAZOLE DERIVATIVES; BIOLOGICAL EVALUATION; MULTISTEP SYNTHESIS; MOLECULAR DOCKING; FACILE SYNTHESIS in [Ma, Fei; Li, Jie; Zhang, Shuning; Gu, Yuang; Tan, Tingting; Chen, Wanting; Wang, Shuyue; Ma, Peixiang; Xu, Hongtao; Yang, Guang] ShanghaiTech Univ, Shanghai Inst Adv Immunochem Studies, Shanghai 201210, Peoples R China; [Lerner, Richard A.] Scripps Res Inst, Dept Chem, La Jolla, CA 92037 USA in 2021, Cited 61. Formula: C8H8O2. The Name is 4-Methoxybenzaldehyde. Through research, I have a further understanding and discovery of 123-11-5
DNA-encoded combinatorial chemical library (DEL) technology, an approach that combines the power of genetics and chemistry, has emerged as an invaluable tool in drug discovery. Skeletal diversity plays a fundamental importance in DEL applications, and relies heavily on novel DNA-compatible chemical reactions. We report herein a phylogenic chemical transformation strategy using DNA-conjugated benzoyl hydrazine as a common versatile precursor in azole chemical expansion of DELs. DNA-compatible reactions deriving from the common benzoyl hydrazine precursor showed excellent functional group tolerance with exceptional efficiency in the synthesis of various azoles, including oxadiazoles, thiadiazoles, and triazoles, under mild reaction conditions. The phylogenic chemical transformation strategy provides DELs a facile way to expand into various unique chemical spaces with privileged scaffolds and pharmacophores.
Formula: C8H8O2. Welcome to talk about 123-11-5, If you have any questions, you can contact Ma, F; Li, J; Zhang, SN; Gu, Y; Tan, TT; Chen, WT; Wang, SY; Ma, PX; Xu, HT; Yang, G; Lerner, RA or send Email.
Reference:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
,Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles